与先天性免疫错误有关的儿童期系统性红斑狼疮:一种还是多种情况?

IF 0.7 4区 医学 Q4 PEDIATRICS Archivos argentinos de pediatria Pub Date : 2025-02-01 Epub Date: 2024-08-29 DOI:10.5546/aap.2024-10370.eng
Mariano N Lorenzo, Dolores Artese, Melina Perdíz, Natalia P Álvarez, Guillermo N Ledo, María V Cohen, Juana I Romero
{"title":"与先天性免疫错误有关的儿童期系统性红斑狼疮:一种还是多种情况?","authors":"Mariano N Lorenzo, Dolores Artese, Melina Perdíz, Natalia P Álvarez, Guillermo N Ledo, María V Cohen, Juana I Romero","doi":"10.5546/aap.2024-10370.eng","DOIUrl":null,"url":null,"abstract":"<p><p>Childhood-onset systemic lupus erythematosus (cSLE) is a multisystem disease; its severity depends on the organs involved. Monogenic diseases have been described as predisposing to the onset of cSLE. Analytical and immunological tests are used for diagnostic confirmation. The main goal of treatment is remission and flare prevention. Here we describe the clinical case of a patient with prolonged febrile syndrome, arthralgias, and anemia, positive analytical tests for antinuclear antibodies and anti-DNA antibodies and low values of complement C3, C4, and C1q; so the patient was diagnosed with cSLE associated with C1q deficiency. Patients with C1q deficiency present with early onset of disease and significant target organ damage with nephritis. An early diagnosis of cSLE is important to ensure an early and appropriate treatment. Treatment may be personalized depending on the underlying defect that generates the subtype of lupus.</p>","PeriodicalId":8338,"journal":{"name":"Archivos argentinos de pediatria","volume":" ","pages":"e202410370"},"PeriodicalIF":0.7000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Childhood-onset systemic lupus erythematosus associated with inborn errors of immunity: One or several conditions?\",\"authors\":\"Mariano N Lorenzo, Dolores Artese, Melina Perdíz, Natalia P Álvarez, Guillermo N Ledo, María V Cohen, Juana I Romero\",\"doi\":\"10.5546/aap.2024-10370.eng\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Childhood-onset systemic lupus erythematosus (cSLE) is a multisystem disease; its severity depends on the organs involved. Monogenic diseases have been described as predisposing to the onset of cSLE. Analytical and immunological tests are used for diagnostic confirmation. The main goal of treatment is remission and flare prevention. Here we describe the clinical case of a patient with prolonged febrile syndrome, arthralgias, and anemia, positive analytical tests for antinuclear antibodies and anti-DNA antibodies and low values of complement C3, C4, and C1q; so the patient was diagnosed with cSLE associated with C1q deficiency. Patients with C1q deficiency present with early onset of disease and significant target organ damage with nephritis. An early diagnosis of cSLE is important to ensure an early and appropriate treatment. Treatment may be personalized depending on the underlying defect that generates the subtype of lupus.</p>\",\"PeriodicalId\":8338,\"journal\":{\"name\":\"Archivos argentinos de pediatria\",\"volume\":\" \",\"pages\":\"e202410370\"},\"PeriodicalIF\":0.7000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archivos argentinos de pediatria\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.5546/aap.2024-10370.eng\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/29 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q4\",\"JCRName\":\"PEDIATRICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archivos argentinos de pediatria","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5546/aap.2024-10370.eng","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/29 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"PEDIATRICS","Score":null,"Total":0}
引用次数: 0

摘要

儿童期发病的系统性红斑狼疮(cSLE)是一种多系统疾病,其严重程度取决于受累器官。据描述,单基因疾病易导致系统性红斑狼疮的发病。分析和免疫学检测可用于确诊。治疗的主要目标是缓解和预防复发。我们在此描述了一个临床病例,该患者伴有长期发热综合征、关节痛和贫血,抗核抗体和抗DNA抗体分析检测呈阳性,补体C3、C4和C1q值偏低,因此被诊断为伴有C1q缺乏症的系统性红斑狼疮。C1q缺乏症患者起病较早,靶器官受损严重,并伴有肾炎。早期诊断系统性红斑狼疮对确保早期和适当的治疗非常重要。治疗可根据导致狼疮亚型的潜在缺陷进行个性化治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Childhood-onset systemic lupus erythematosus associated with inborn errors of immunity: One or several conditions?

Childhood-onset systemic lupus erythematosus (cSLE) is a multisystem disease; its severity depends on the organs involved. Monogenic diseases have been described as predisposing to the onset of cSLE. Analytical and immunological tests are used for diagnostic confirmation. The main goal of treatment is remission and flare prevention. Here we describe the clinical case of a patient with prolonged febrile syndrome, arthralgias, and anemia, positive analytical tests for antinuclear antibodies and anti-DNA antibodies and low values of complement C3, C4, and C1q; so the patient was diagnosed with cSLE associated with C1q deficiency. Patients with C1q deficiency present with early onset of disease and significant target organ damage with nephritis. An early diagnosis of cSLE is important to ensure an early and appropriate treatment. Treatment may be personalized depending on the underlying defect that generates the subtype of lupus.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
1.40
自引率
25.00%
发文量
286
审稿时长
6-12 weeks
期刊介绍: Archivos Argentinos de Pediatría is the official publication of the Sociedad Argentina de Pediatría (SAP) and has been published without interruption since 1930. Its publication is bimonthly. Archivos Argentinos de Pediatría publishes articles related to perinatal, child and adolescent health and other relevant disciplines for the medical profession.
期刊最新文献
Fiber in enteral nutrition: why and what for? [Recommendations on the use of palivizumab: update 2023]. Liver transplantation for primary liver tumors in pediatrics. A case series. The diagnosis of short lingual frenulum and how to promote breastfeeding. The lingual frenulum, ankyloglossia, and breastfeeding.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1